Instituto de Química Médica (CSIC), Juan de la Cierva, 3, E-28006 Madrid, Spain.
J Chem Phys. 2011 Sep 14;135(10):104116. doi: 10.1063/1.3632086.
The set of 1:1 and 2:1 complexes of XOOX' (X, X' = H, CH(3)) with lithium cation has been studied to determine if they are suitable candidates for chiral discrimination in an isotropic medium via nuclear magnetic resonance spectroscopy. Conventional nuclear magnetic resonance is unable to distinguish between enantiomers in the absence of a chiral solvent. The criterion for experimental detection is valuated by the isotropic part of nuclear shielding polarisability tensors, related to a pseudoscalar of opposite sign for two enantiomers. The study includes calculations at coupled Hartree-Fock and density functional theory schemes for (17)O nucleus in each compound. Additional calculations for (1)H are also included for some compounds. A huge static homogeneous electric field, perpendicular to the magnetic field of the spectromer, as big as ≈1.7 × 10(8) V m(-1) should be applied to observe a shift of ≈1 ppm for (17)O magnetic shielding in the proposed set of complexes.
已研究了 XOOX'(X、X'=H、CH(3))与锂离子的 1:1 和 2:1 配合物,以确定它们是否适合通过各向同性中的核磁共振光谱法在手性介质中进行手性分辨。在没有手性溶剂的情况下,常规核磁共振无法区分对映异构体。实验检测的标准是通过与两个对映异构体相反符号的赝标量相关的核屏蔽极化张量的各向同性部分来评估的。该研究包括在每个化合物中的(17)O 核的耦合 Hartree-Fock 和密度泛函理论方案中的计算。对于一些化合物,还包括对(1)H 的额外计算。应施加一个与光谱仪磁场垂直的巨大静态均匀电场,大小约为 ≈1.7 × 10(8) V m(-1),以便观察在所提出的配合物集中,(17)O 磁屏蔽的 ≈1 ppm 位移。